International CIPN Assessment and Validation Study (NCT04633655)
International Chemotherapy Induced Peripheral Neurotoxicity (CIPN) Assessment and Validation Study
🩺 Plain-English Summary (8th-Grade Level)
This is an observational study of chemotherapy-induced peripheral neurotoxicity (CIPN) patients to be investigated prospectively in order to assess responsiveness of a set of outcome measures in an international multi-center study.
Who can join: Review the eligibility criteria below.
Location: Birmingham School of Nursing, University of Alabama — Birmingham, Alabama
Age range: 18 Years
🧪 Interventions in This Study
- outcome measures for CIPN testing (OTHER)
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (30 Sites)
Showing the first 25 of 30 sites.
- Birmingham School of Nursing, University of Alabama — Birmingham, Alabama
- Northside Hospital — Atlanta, Georgia
- JHU — Baltimore, Maryland
- University of Michigan School of Nursing — Ann Arbor, Michigan
- Columbia University Irving Medical Center — New York, New York
- Cancer Center/Wexner Medical Center - Ohio State Medical Oncology Division — Columbus, Ohio
- Dartmouth-Hitchcock Medical Center — Lebanon, Pennsylvania
- University of Vermont Medical Center — Burlington, Vermont
- Brain and Mind Center — Sydney,
- Dept. of Neurology, Medical University of Vienna — Vienna,
- International Centre for Diarrhoeal Disease Research — Dhaka,
- Clínica AMO — Salvador,
- The Ottawa Hospital — Ottawa,
- Aarhus University Hospital — Aarhus,
- Hôpital Percy — Clamart,
- CHU Dupuytren — Limoges,
- Center for Molecular Medicine — Cologne,
- University of Larissa — Larissa,
- "Saint Andrew's" State General Hospital — Pátrai,
- San Gerardo Hospital — Monza, Mb
- Ospedale Valduce — Como,
- Ospedale Policlinico San Martino — Genova,
- A.O.U. Policlinico "G. Martino" — Messina,
- Padova Hospital — Padova,
- Azienda Ospedaliera Universitaria — Verona,
📞 Contact the Study Coordinator
Phone: + 39 02 6448 8039
Email: guido.cavaletti@unimib.it
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Chemotherapy-induced Peripheral Neuropathy
- The Effect of Electroacupuncture on Nerve Pain Caused by Chemotherapy (Chemotherapy-Induced Peripheral Neuropathy) — Boston, Massachusetts
- NIAGEN and Persistent Chemotherapy-Induced Peripheral Neuropathy — Iowa City, Iowa
- Exercise-based Rehabilitation to Treat Persistent Chemotherapy Induced Peripheral Neuropathy (CIPN) — Toronto, Ontario
- Efficacy and Safety of ATX01 in Adult Patients With CIPN (Chemotherapy-induced Peripheral Neuropathy) — Clermont, Florida
- Duloxetine and Neurofeedback Training for the Treatment of Chemotherapy Induced Peripheral Neuropathy — Houston, Texas
- PEA for the Relief of Chemotherapy-Induced Peripheral Neuropathy — Middletown, Connecticut
Explore by condition: All Chemotherapy-induced Peripheral Neuropathy clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.